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Boron and Nitrogen Co‐Doped Trimodal‐Porous Wood‐Derived Carbon for Boosting Capacitive Performance

Authors :
Liu, Kun
Xu, Jijian
Wang, Yuan
Qian, Meng
Zhao, Wei
Zeng, Yi
Huang, Fuqiang
Source :
Energy Technology; January 2020, Vol. 8 Issue: 1
Publication Year :
2020

Abstract

Heteroatom doping and a porous structure are two significant factors that improve the capacitance performance of carbon‐based electrodes, but there are often one‐sided considerations between them. Herein, effective B, N co‐doping and trimodal‐porous structure from the carbonization of sustainable natural wood are obtained at the same time. The unique pore structure is coarsely tuned by a modified ZnAc2‐assisted hypersaline route and further fine‐tuned by controlling the doping levels of boron and nitrogen. The high specific surface area of porous carbon up to 1201 m2g−1is coordinated with the trimodal foam‐like nanopores. This carbon‐based material as a supercapacitor electrode can provide not only trimodal‐porous ion transfer highways but also doping‐induced pseudocapacitance. The resulting pore and heteroatom reengineered wood‐derived carbon harvests a remarkable capacitance of 479 F g−1at 1 A g−1, among the highest values in reported B, N co‐doped carbon electrodes. The aqueous symmetric supercapacitor exhibits energy density of 18.5 Wh kg−1and power density of 6.4 kW kg−1, along with >90% capacitance retention, both in H2SO4and Li2SO4electrolyte over 10 000 cycles. Wood‐derived carbon, integrating B, N co‐doping, and a trimodal‐porous structure, are obtained from a green modified hypersaline route. The resulting pore and heteroatom reengineered porous carbon harvests a remarkable specific capacitance of 479 F g−1and high energy density of 18.5 Wh kg−1, as well as good rate capability in aqueous supercapacitors.

Details

Language :
English
ISSN :
21944288 and 21944296
Volume :
8
Issue :
1
Database :
Supplemental Index
Journal :
Energy Technology
Publication Type :
Periodical
Accession number :
ejs52022379
Full Text :
https://doi.org/10.1002/ente.201900950